| Literature DB >> 36070756 |
Nicholas Borcherding1, Wentong Jia2, Rocky Giwa2, Rachael L Field2, John R Moley2, Benjamin J Kopecky3, Mandy M Chan4, Bin Q Yang3, Jessica M Sabio5, Emma C Walker6, Omar Osorio3, Andrea L Bredemeyer3, Terri Pietka3, Jennifer Alexander-Brett4, Sharon Celeste Morley7, Maxim N Artyomov2, Nada A Abumrad8, Joel Schilling4, Kory Lavine9, Clair Crewe8, Jonathan R Brestoff10.
Abstract
Adipocytes transfer mitochondria to macrophages in white and brown adipose tissues to maintain metabolic homeostasis. In obesity, adipocyte-to-macrophage mitochondria transfer is impaired, and instead, adipocytes release mitochondria into the blood to induce a protective antioxidant response in the heart. We found that adipocyte-to-macrophage mitochondria transfer in white adipose tissue is inhibited in murine obesity elicited by a lard-based high-fat diet, but not a hydrogenated-coconut-oil-based high-fat diet, aging, or a corn-starch diet. The long-chain fatty acids enriched in lard suppress mitochondria capture by macrophages, diverting adipocyte-derived mitochondria into the blood for delivery to other organs, such as the heart. The depletion of macrophages rapidly increased the number of adipocyte-derived mitochondria in the blood. These findings suggest that dietary lipids regulate mitochondria uptake by macrophages locally in white adipose tissue to determine whether adipocyte-derived mitochondria are released into systemic circulation to support the metabolic adaptation of distant organs in response to nutrient stress.Entities:
Keywords: CD36; EXT1; aging; beige fat; brown adipose tissue; cell-free mitochondria; fatty acids; heparan sulfate; horizontal mitochondria transfer; intercellular mitochondria transfer; lipids; macrophage; mitochondria; obesity; palmitate; white adipose tissue
Mesh:
Substances:
Year: 2022 PMID: 36070756 PMCID: PMC9547954 DOI: 10.1016/j.cmet.2022.08.010
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 31.373